- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT00017225
Chemotherapy and Radiation Therapy With or Without Peripheral Stem Cell Transplantation in Treating Patients With Neuroblastoma
Neuroblastoma Study Phase II Study of Various Therapies in Patients With Neuroblastoma
RATIONALE: Drugs used in chemotherapy use different ways to stop tumor cells from dividing so they stop growing or die. Radiation therapy uses high-energy x-rays to damage tumor cells. Peripheral stem cell transplantation may be able to replace immune cells that were destroyed by chemotherapy or radiation therapy used to kill tumor cells. Combining these therapies may kill more tumor cells.
PURPOSE: Phase II trial to study the effectiveness of combining chemotherapy and radiation therapy with or without peripheral stem cell transplantation in treating patients who have neuroblastoma.
Study Overview
Status
Conditions
Intervention / Treatment
- Drug: carboplatin
- Drug: cyclophosphamide
- Radiation: radiation therapy
- Drug: etoposide
- Drug: vincristine sulfate
- Drug: cisplatin
- Drug: doxorubicin hydrochloride
- Procedure: conventional surgery
- Procedure: peripheral blood stem cell transplantation
- Biological: filgrastim
- Procedure: autologous bone marrow transplantation
- Drug: melphalan
- Drug: tretinoin
- Drug: dacarbazine
- Drug: ifosfamide
- Drug: vindesine
Detailed Description
OBJECTIVES:
- Determine the frequency of spontaneous remission in pediatric patients with localized neuroblastoma.
- Determine the course of regression in patients with spontaneous remission.
- Determine the event-free survival rate of patients with high-risk neuroblastoma treated with maintenance chemotherapy OR consolidation chemotherapy followed by autologous stem cell rescue.
- Determine if a correlation exists between long-term overall survival and catecholamine response in these high-risk patients.
- Determine if a correlation exists between cytotoxic and conditioning chemotherapies, in terms of bone marrow toxicity, in these high-risk patients.
OUTLINE: This is a multicenter study. Patients are stratified according to risk (low vs standard vs high).
- Observation stratum (low risk): Patients undergo surgical biopsy followed by observation for 6-12 months. Patients may also undergo second-look surgery. Patients with tumor regression receive no further therapy. Patients with disease progression or no tumor regression receive standard-risk chemotherapy as in the standard-risk stratum.
- Standard-risk stratum: Patients undergo surgical biopsy. Patients at least 6 months of age receive 1 course of chemotherapy comprising cisplatin IV and etoposide IV continuously on days 1-4 and vindesine IV over 1 hour on day 1. Patients then receive 1 course of chemotherapy comprising vincristine IV over 1 hour on days 1 and 8, dacarbazine IV over 1 hour on days 1-5, ifosfamide IV continuously on days 1-5, and doxorubicin IV over 4 hours on days 6 and 7.
Patients under 6 months of age receive doxorubicin IV over 30 minutes and vincristine IV on days 1, 3, and 5 and cyclophosphamide IV over 5 minutes on days 1-7. Treatment repeats every 3 weeks for 2 courses in the absence of unacceptable toxicity.
After chemotherapy, patients may undergo second-look surgery followed by 2 additional courses of chemotherapy as above. Patients with complete response or very good partial response receive no further therapy. Patients with partial response, minimal response, no response, or progressive disease undergo local radiotherapy daily 5 days a week for approximately 6 weeks. Patients with no response after radiotherapy may then receive therapy as in the high-risk stratum.
- High-risk stratum: Patients undergo surgical biopsy. Patients at least 6 months of age receive induction chemotherapy comprising cisplatin, etoposide, and vindesine as in the standard-risk stratum combined with filgrastim (G-CSF) subcutaneously (SC) daily beginning on day 8 and continuing until blood counts recover. Patients also receive alternating courses of vincristine, dacarbazine, ifosfamide, and doxorubicin as in the standard-risk stratum combined with G-CSF SC daily beginning on day 9 and continuing until blood counts recover. Treatment repeats every 3 weeks for up to 6 courses in the absence of unacceptable toxicity.
Patients under 6 months of age receive 2 courses of induction chemotherapy as in the standard-risk stratum followed by 4 courses of alternating chemotherapy as above.
Patients may also undergo second-look surgery.
Patients then receive consolidation chemotherapy comprising melphalan IV over 30 minutes on days -8 to -5, etoposide IV over 4 hours on day -4, and carboplatin IV over 1 hour on days -4 to -2. Patients undergo autologous stem cell transplantation (ASCT) on day 0. Patients also receive G-CSF SC or IV over 2 hours daily beginning on day 0. Patients may then undergo radiotherapy daily 5 days a week for 6 weeks.
Patients who were diagnosed less than 1 year ago and who do not demonstrate MYCN amplication receive maintenance chemotherapy comprising oral cyclophosphamide on days 1-8 (instead of consolidation chemotherapy and ASCT as above). Treatment repeats every 3 weeks for 4 courses.
Beginning 4-6 weeks after transplantation or 4 weeks after initiation of the last course of maintenance chemotherapy, all patients receive consolidation therapy with oral tretinoin 3 times daily on days 1-14. Treatment repeats every 28 days for 6 courses followed by a 3-month rest. Patients then receive 3 additional courses.
Patients are followed at 6 weeks, every 3 months for 5 years, and then every 6 months thereafter.
PROJECTED ACCRUAL: Approximately 130 patients (50 in high-risk stratum, 15 in standard-risk stratum, and 65 in observation stratum) will be accrued for this study within 1 year.
Study Type
Phase
- Phase 2
Contacts and Locations
Study Locations
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Aachen, Germany, D-52074
- Urologische Klinik - Universitaetsklinikum Aachen
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Augsburg, Germany, DOH-86156
- Zentralklinikum Augsburg
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Augsburg, Germany, 86154
- Kinderkrankenhaus Josefinum
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Bad Mergentheim, Germany, 97980
- Caritaskrankenhaus
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Bayreuth, Germany, 95445
- Klinikum Bayreuth
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Berlin, Germany, D-13353
- Charité - Campus Virchow Klinikum
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Berlin, Germany, 13122
- Helios Klinikum Berlin
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Biefeld, Germany, 33617
- Krankenanstalten Gilead
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Bonn, Germany, DOH-53113
- Kinderklinik der Universitaet-Bonn
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Braunschweig, Germany, 38118
- Stadt Klinikum - Howedestrase
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Bremen, Germany, D-28205
- Zentralkrankenhaus
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Chemnitz, Germany, D-09116
- Klinikum Chemnitz GmbH
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Coburg, Germany, 96450
- Klinikum Coburg
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Cologne, Germany, D-50924
- Medizinische Universitaetsklinik I
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Cottbus, Germany, D-03048
- Carl - Thiem - Klinkum Cottbus
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Datteln, Germany, 45704
- Vestische Kinderklinik
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Detmold, Germany, 32756
- Klinikum Lippe - Detmold
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Dortmund, Germany, 44123
- Stadt. Kliniken
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Dresden, Germany, D-01307
- Universitatsklinikum Carl Gustav Carl Carus
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Dresden, Germany, 01229
- Stadt. KH Dresden - Neustadt
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Duesseldorf, Germany, D-40225
- Universitaetsklinik Duesseldorf
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Erfurt, Germany, 99012
- HELIOS Klinikum Erfurt GmbH
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Erlangen, Germany, D-91054
- Universitaets - Kinderklinik
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Essen, Germany, D-45122
- Universitaetsklinikum Essen
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Frankfurt, Germany, D-60590
- Klinikum der J.W. Goethe Universitaet
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Freiburg, Germany, 79106
- Universitaetskinderklinik - Universitaetsklinikum Freiburg
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Gelsenkirchen, Germany, 45892
- Stadt. Kinderklinik
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Giessen, Germany, D-35385
- Kinderklinik
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Goettingen, Germany, D-37075
- Universitaetsklinikum Goettingen
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Greiswald, Germany, 17487
- Universitats - Kinderklinik
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Gummersbach, Germany, D-51643
- Kreiskrankenhaus Gummersbach GmbH
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Halle, Germany, 06003
- St. Barbara Krankenhaus
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Halle, Germany, 06097
- Martin Luther Universitaet
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Hamburg, Germany, D-20246
- Universitaets-Krankenhaus Eppendorf
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Hamburg, Germany, 22763
- Altonaer Kinderkrankenhaus
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Hamm, Germany, DOH-59063
- Evangelische Krankenhaus Hamm
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Hannover, Germany, D-30625
- Medizinische Hochschule Hannover
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Hannover, Germany, 30173
- Kinderkrankenhaus auf der Bult
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Heidelberg, Germany, D-69120
- Universitaets-Kinderklinik Heidelberg
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Herdecke, Germany, 58313
- Gemeinschaftskrankenhaus
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Homburg, Germany, 66421
- Universitatsklinik Homburg
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Homburg, Germany, D-66421
- Marien Hospital
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Iserlohn, Germany, D-58644
- Praxis am Evangelischen Krankenhaus Bethanien
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Jena, Germany, D-07745
- Universitaets - Kinderklinik
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Kaiserslautern, Germany, D-67653
- Westpfalz-Klinikum GmbH
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Karlsruhe, Germany, 76131
- Stadt. Kinderklinik
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Kassel, Germany, D-34125
- Klinikum Kassel
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Kassel, Germany, 34121
- Kinderkrankenhaus
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Kiel, Germany, D-24105
- University Hospital Schleswig-Holstein - Kiel Campus
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Kiel, Germany, 23116
- Staedtische Krankenhaus Kiel
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Koblenz, Germany, 56065
- Stadt. Krankenhaus Kemperhof
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Koln - Riehl, Germany, D-50735
- Staedtisches Kinderkrankenhaus
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Konstanz, Germany, 78461
- Klinik Konstanz
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Krefeld, Germany, D-47805
- Klinikum Krefeld GmbH
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Leipzig, Germany, 04317
- Universitaets - Kinderklinik
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Leipzig, Germany, D-04317
- Universitaets Klinik fuer Kinderchirurgie
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Lubeck, Germany, 23538
- Universitaets - Kinderklinik - Luebeck
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Ludwigshafen, Germany, 67065
- St. Annastift Krankenhaus
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Magdeburg, Germany, 39112
- Universitatsklinikum der MA
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Mainz, Germany, D-55131
- Johannes Gutenberg University
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Mannheim, Germany, 68167
- Stadt. Klinik - Kinderklinik
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Marburg, Germany, 35033
- Universitaets - Kinderklinik
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Minden, Germany, D-32423
- Klinikum Minden
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Muenster, Germany, D-48149
- Klinik und Poliklinik fuer Kinderheilkunde - Universitaetsklinikum Muenster
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Munich, Germany, D-81545
- Staedtisches Krankenhaus Muenchen - Harlaching
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Munich, Germany, 80336
- Universitaets - Kinderpoliklinik
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Munich, Germany, 80804
- Kinderklinik d. TU / Schwabing
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Munich, Germany, DOH-80337
- Kinderklinik
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Neunkirchen, Germany, 66539
- Kinderklinik Kohlhof
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Nuernberg, Germany, 90419
- Cnopfche Kinderklinik
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Oldenburg, Germany, 26133
- Klinikum Oldenburg
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Osnabruck, Germany, D-49082
- Kindershospital
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Regensburg, Germany, 93049
- Krankenhaus D Barmherzigen Brueder
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Rosenheim, Germany, 83022
- Staedtische Klinikum-Kinderklinik
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Rostock, Germany, D-18057
- Kinderklinik - Universitaetsklinikum Rostock
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Saarbrucken, Germany, 66119
- Saarbrucker Winterbergkliniken
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Schwabisch Hall, Germany, 74523
- Diakone - Krankenhaus
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Schwerin, Germany, D-19049
- Klinikum Schwerin
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Schwienfurt, Germany, 97422
- Leopoldina - Krankenhaus
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Siegen, Germany, 57072
- Deutsches Rotes Kreuz
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St. Augustin, Germany, 53757
- Johanniter-Kinderklinik
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Stuttgart, Germany, DOH-70176
- Olgahospital
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Trier, Germany, D-54290
- Mutterhaus der Borromäerinnen
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Tuebingen, Germany, D-72076
- Universitaetsklinikum Tuebingen
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Ulm, Germany, D-89075
- Universitaet Ulm
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Vechta, Germany, D-49377
- St. Marien Hospital
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Wilhelmshaven, Germany, 26389
- Reinhard - Nieter - Krankenhaus
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Wuerzburg, Germany, D-97080
- Universitaets - Kinderklinik Wuerzburg
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Wuppertal, Germany, D-42283
- Helios Klinikum Wuppertal
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Maastricht, Netherlands, 6202 AZ
- Academisch Ziekenhuis Maastricht
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Basel, Switzerland, CH-4005
- University Children's Hospital
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Locarno, Switzerland, 6600
- Ospedale "la Carita", Locarno
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Luzerne 16, Switzerland, CH-6000
- Kinderspital Luzerne
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Zurich, Switzerland, CH-8032
- University Children's Hospital
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
DISEASE CHARACTERISTICS:
- Histologically confirmed neuroblastoma
Observation stratum:
- MYCN gene not amplified
- Infants with stage I-IVS disease OR
- Over 1 year of age and stage I or II resectable disease
Standard-risk stratum:
- MYCN gene not amplified
- Infants with serious symptoms and stage II-IVS disease OR
- Over 1 year of age with stage II or III unresectable disease
High-risk stratum:
- Stage IV disease OR
- Stage I-IVS MYCN gene-amplified disease
PATIENT CHARACTERISTICS:
Age:
- 20 and under
Performance status:
- Not specified
Life expectancy:
- Not specified
Hematopoietic:
- Not specified
Hepatic:
- Not specified
Renal:
- No kidney insufficiency
Cardiovascular:
- No cardiac insufficiency
Other:
- Not pregnant
- Fertile patients must use effective contraception
- No other serious illness
PRIOR CONCURRENT THERAPY:
Biologic therapy:
- Not specified
Chemotherapy:
- No prior chemotherapy within 6 months after diagnosis
Endocrine therapy:
- Not specified
Radiotherapy:
- Not specified
Surgery:
- Not specified
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
Collaborators and Investigators
Investigators
- Study Chair: Frank Berthold, MD, Children's Hospital Medical Center, Cincinnati
Publications and helpful links
General Publications
- Decarolis B, Simon T, Krug B, Leuschner I, Vokuhl C, Kaatsch P, von Schweinitz D, Klingebiel T, Mueller I, Schweigerer L, Berthold F, Hero B. Treatment and outcome of Ganglioneuroma and Ganglioneuroblastoma intermixed. BMC Cancer. 2016 Jul 27;16:542. doi: 10.1186/s12885-016-2513-9.
- Hero B, Simon T, Spitz R, Ernestus K, Gnekow AK, Scheel-Walter HG, Schwabe D, Schilling FH, Benz-Bohm G, Berthold F. Localized infant neuroblastomas often show spontaneous regression: results of the prospective trials NB95-S and NB97. J Clin Oncol. 2008 Mar 20;26(9):1504-10. doi: 10.1200/JCO.2007.12.3349.
- Krams M, Hero B, Berthold F, Parwaresch R, Harms D, Rudolph P. Proliferation marker KI-S5 discriminates between favorable and adverse prognosis in advanced stages of neuroblastoma with and without MYCN amplification. Cancer. 2002 Feb 1;94(3):854-61.
- Simon T, Hero B, Dupuis W, Selle B, Berthold F. The incidence of hearing impairment after successful treatment of neuroblastoma. Klin Padiatr. 2002 Jul-Aug;214(4):149-52. doi: 10.1055/s-2002-33179.
- Spitz R, Hero B, Westermann F, Ernestus K, Schwab M, Berthold F. Fluorescence in situ hybridization analyses of chromosome band 1p36 in neuroblastoma detect two classes of alterations. Genes Chromosomes Cancer. 2002 Jul;34(3):299-305. doi: 10.1002/gcc.10070.
- Simon T, Hero B, Benz-Bohm G, von Schweinitz D, Berthold F. Review of image defined risk factors in localized neuroblastoma patients: Results of the GPOH NB97 trial. Pediatr Blood Cancer. 2008 May;50(5):965-9. doi: 10.1002/pbc.21343.
- Berthold F, Hero B, Kremens B, Handgretinger R, Henze G, Schilling FH, Schrappe M, Simon T, Spix C. Long-term results and risk profiles of patients in five consecutive trials (1979-1997) with stage 4 neuroblastoma over 1 year of age. Cancer Lett. 2003 Jul 18;197(1-2):11-7. doi: 10.1016/s0304-3835(03)00076-4.
- Spitz R, Hero B, Ernestus K, Berthold F. Deletions in chromosome arms 3p and 11q are new prognostic markers in localized and 4s neuroblastoma. Clin Cancer Res. 2003 Jan;9(1):52-8.
- Spitz R, Hero B, Ernestus K, Berthold F. FISH analyses for alterations in chromosomes 1, 2, 3, and 11 define high-risk groups in neuroblastoma. Med Pediatr Oncol. 2003 Jul;41(1):30-5. doi: 10.1002/mpo.10313.
- Spitz R, Hero B, Ernestus K, Berthold F. Gain of distal chromosome arm 17q is not associated with poor prognosis in neuroblastoma. Clin Cancer Res. 2003 Oct 15;9(13):4835-40.
- von Schweinitz D, Hero B, Berthold F. The impact of surgical radicality on outcome in childhood neuroblastoma. Eur J Pediatr Surg. 2002 Dec;12(6):402-9. doi: 10.1055/s-2002-36952.
- Simon T, Hero B, Bongartz R, Schmidt M, Muller RP, Berthold F. Intensified external-beam radiation therapy improves the outcome of stage 4 neuroblastoma in children > 1 year with residual local disease. Strahlenther Onkol. 2006 Jul;182(7):389-94. doi: 10.1007/s00066-006-1498-8.
- Kremens B, Hero B, Esser J, Weinel P, Filger-Brillinger J, Fleischhack G, Graf N, Gruttner HP, Niemeyer C, Schulz A, Wickmann L, Berthold F. Ocular symptoms in children treated with human-mouse chimeric anti-GD2 mAb ch14.18 for neuroblastoma. Cancer Immunol Immunother. 2002 Apr;51(2):107-10. doi: 10.1007/s00262-001-0259-x. Epub 2002 Feb 1.
Study record dates
Study Major Dates
Study Start
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Estimate)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
- Neoplasms by Histologic Type
- Neoplasms
- Neoplasms, Glandular and Epithelial
- Neoplasms, Neuroepithelial
- Neuroectodermal Tumors
- Neoplasms, Germ Cell and Embryonal
- Neoplasms, Nerve Tissue
- Neuroectodermal Tumors, Primitive
- Neuroectodermal Tumors, Primitive, Peripheral
- Neuroblastoma
- Physiological Effects of Drugs
- Molecular Mechanisms of Pharmacological Action
- Enzyme Inhibitors
- Antirheumatic Agents
- Antineoplastic Agents
- Immunosuppressive Agents
- Immunologic Factors
- Tubulin Modulators
- Antimitotic Agents
- Mitosis Modulators
- Antineoplastic Agents, Alkylating
- Alkylating Agents
- Myeloablative Agonists
- Antineoplastic Agents, Phytogenic
- Topoisomerase II Inhibitors
- Topoisomerase Inhibitors
- Dermatologic Agents
- Antibiotics, Antineoplastic
- Keratolytic Agents
- Cyclophosphamide
- Carboplatin
- Etoposide
- Ifosfamide
- Melphalan
- Doxorubicin
- Liposomal doxorubicin
- Vincristine
- Dacarbazine
- Tretinoin
- Vindesine
Other Study ID Numbers
- GPOH-GERMANY-NB97
- CDR0000068664 (Registry Identifier: PDQ (Physician Data Query))
- EU-20102
- GER-GPOH-NB97
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
Clinical Trials on Neuroblastoma
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Children's Oncology GroupNational Cancer Institute (NCI)Active, not recruitingStage 4S Neuroblastoma | Ganglioneuroblastoma | Stage 2A Neuroblastoma | Stage 2B Neuroblastoma | Stage 3 Neuroblastoma | Stage 4 Neuroblastoma | Stage 1 Neuroblastoma | Stage 2 NeuroblastomaUnited States, Canada, Australia, New Zealand
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Children's Oncology GroupNational Cancer Institute (NCI)CompletedRecurrent Neuroblastoma | Disseminated Neuroblastoma | Localized Resectable Neuroblastoma | Localized Unresectable Neuroblastoma | Regional Neuroblastoma | Stage 4S NeuroblastomaUnited States
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Children's Oncology GroupNational Cancer Institute (NCI)Active, not recruitingLocalized Resectable Neuroblastoma | Localized Unresectable Neuroblastoma | Regional Neuroblastoma | Stage 4S Neuroblastoma | Ganglioneuroblastoma | Stage 4 NeuroblastomaUnited States
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Children's Oncology GroupNational Cancer Institute (NCI)Active, not recruitingRecurrent Neuroblastoma | Stage 4S Neuroblastoma | Stage 2A Neuroblastoma | Stage 2B Neuroblastoma | Stage 3 Neuroblastoma | Stage 4 NeuroblastomaUnited States, Canada, Australia, New Zealand
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National Cancer Institute (NCI)Active, not recruitingRecurrent Neuroblastoma | Localized Resectable Neuroblastoma | Localized Unresectable Neuroblastoma | Regional Neuroblastoma | Stage 4S Neuroblastoma | Stage 4 NeuroblastomaUnited States, Canada, Australia, New Zealand, Puerto Rico
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Children's Oncology GroupNational Cancer Institute (NCI)CompletedRecurrent Neuroblastoma | Localized Resectable Neuroblastoma | Localized Unresectable Neuroblastoma | Regional Neuroblastoma | Stage 4S Neuroblastoma | Stage 4 NeuroblastomaUnited States, Canada, Australia, New Zealand, Puerto Rico, Switzerland
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Children's Oncology GroupNational Cancer Institute (NCI)RecruitingLocalized Resectable Neuroblastoma | Localized Unresectable Neuroblastoma | Regional Neuroblastoma | Stage 4S Neuroblastoma | Ganglioneuroblastoma | Stage 4 NeuroblastomaUnited States, Puerto Rico, Canada, Australia, New Zealand, Netherlands, Saudi Arabia, Switzerland
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Children's Oncology GroupNational Cancer Institute (NCI)CompletedRecurrent Neuroblastoma | Localized Resectable Neuroblastoma | Localized Unresectable Neuroblastoma | Regional Neuroblastoma | Stage 4 NeuroblastomaUnited States
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Children's Oncology GroupNational Cancer Institute (NCI)CompletedLocalized Resectable Neuroblastoma | Localized Unresectable Neuroblastoma | Regional Neuroblastoma | Stage 4S NeuroblastomaUnited States
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Children's Oncology GroupNational Cancer Institute (NCI)CompletedRecurrent Neuroblastoma | Disseminated Neuroblastoma | Localized Resectable Neuroblastoma | Localized Unresectable Neuroblastoma | Stage 4S NeuroblastomaUnited States
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